Build what clinicalresearch runs on.
We are a small team in Gurugram building the EDC and the unified eClinical platform behind it. If you have run trials, or want to build software that people running trials depend on, we would like to talk.
What the work actually looks like.
Built by people who ran trials
Data managers who have shipped a database lock sit next to the engineers building the thing. Neither side translates through a spec.
Work that reaches real sites
What you ship gets used by coordinators from metro hospitals to district sites — where connectivity is unreliable and the data still has to be right.
Small team, real ownership
You own a surface end to end. No layer of product managers between you and the people whose day your work changes.
Open roles.
Open a role to read the detail, then apply straight through WhatsApp — no form, no login, no ATS black hole.
Clinical Data Manager
Clinical OperationsGurugram · HybridFull-timeRead moreClose
Clinical Data Manager
Own study build and data quality for bioequivalence and Phase II studies running on Trialion — and shape the product from inside the work it supports.
What you will do
- Build eCRFs, edit checks, and visit schedules for BA-BE and Phase II protocols
- Run data review, query management, and reconciliation through to database lock
- Write and execute the protocol-specific PQ that ships with each study
- Turn recurring manual work into product requirements our engineers can build
What you will bring
- 3+ years in clinical data management at a CRO or sponsor
- Hands-on study build in at least one EDC (Medidata, Oracle, Octalsoft, Castor, or similar)
- Working knowledge of CDSCO Schedule Y, Indian GCP, and CDISC ODM / SDTM
- Comfort explaining a data problem to engineers who have never run a trial
Senior Frontend Engineer
EngineeringGurugram · Hybrid or RemoteFull-timeRead moreClose
Senior Frontend Engineer
Build the interfaces data managers and coordinators live in all day — the eCRF designer, the data-review workspace, and capture that holds up on a patchy connection at a district hospital.
What you will do
- Ship product surfaces in React and TypeScript against a regulated backend
- Build the drag-and-drop eCRF designer and the query-resolution workspace
- Make offline-first capture behave predictably when connectivity is unreliable
- Hold the line on accessibility and performance on low-end site hardware
What you will bring
- 4+ years building production React with TypeScript
- Real experience with complex forms, tables, and state — not just marketing pages
- An eye for the difference between a demo and something a coordinator can use at 9pm
- Regulated-industry experience is welcome but not required
Backend Engineer, Platform
EngineeringGurugram · Hybrid or RemoteFull-timeRead moreClose
Backend Engineer, Platform
Own the data model and audit trail every module writes into — the part of the platform that has to be right, because a regulator will read it.
What you will do
- Design and extend the unified trial data model behind every module
- Build the immutable audit trail and electronic-signature paths
- Ship the integration layer: central labs, HIS feeds, CTRI, safety databases
- Keep exports submission-grade — CDISC ODM / SDTM without re-mapping
What you will bring
- 4+ years building backend services and relational data models
- Care about correctness, migrations, and data you cannot silently lose
- API design experience against messy third-party systems
- Interest in what 21 CFR Part 11 actually asks of software
CSV & Validation Engineer
Quality & ComplianceGurugram · On-siteFull-timeRead moreClose
CSV & Validation Engineer
Own computerised system validation end to end, so every environment ships audit-ready and QA teams re-run only the protocol-specific PQ.
What you will do
- Author and maintain IQ / OQ / PQ documentation and the validation pack
- Run release validation and keep the traceability matrix current
- Support customer QA teams and Indian GCP audits with evidence, fast
- Fold validation into the engineering workflow instead of bolting it on at the end
What you will bring
- 3+ years in CSV or QA within a GxP-regulated software or CRO environment
- Working knowledge of 21 CFR Part 11, ICH E6(R3), and GAMP 5
- Precise technical writing — the kind an inspector can follow
- Willingness to automate the parts of validation that should not be manual
Implementation Consultant
Customer SuccessGurugram · Some travel to sitesFull-timeRead moreClose
Implementation Consultant
Take CROs from signature to first patient in — migrations, study build, site training — and stay close enough to know what breaks in the real world.
What you will do
- Run migrations from Octalsoft, Castor, MaxisIT, Datatrak, or paper and Excel
- Configure first studies with customer data managers and train site coordinators
- Be the escalation path during study start-up and through database lock
- Bring recurring friction back to product with evidence attached
What you will bring
- 3+ years in clinical operations, data management, or eClinical implementation
- Confidence in front of a room of site coordinators, wherever the site is
- Enough technical depth to debug an integration before escalating it
- Willingness to travel to sites
Nothing here fits, but you think you should be here?
Tell us what you do and what you would want to own. We read every message, and we hire ahead of a posting when the person is right.
+91 73570 17420